At Panacea we believe in a better way of doing things. Everyone talks about delivering a fresh, dynamic, approach – but at Panacea we deliver on this promise. Our highly experienced team enjoy working with clients to find the best way to safeguard their investment and reputation, and we take pride in providing the best possible vigilance services to the pharmaceutical industry. Currently, Panacea are responsible for Marketing Authorisation’s in every EU country and have an international reputation which is respected by regulators.

• A Qualified Person responsible for
  Pharmacovigilance (QPPV) 

• Safety Physician Services 

• Full and ad hoc PV services including:
  • Weekly Literature Monitoring
  • Safety Data Exchange Agreements (SDEAs)
  • Risk Management Plans (RMPs)
  • Creation and Maintenance of Pharmacovigilance
    Safety Master Files (PSMFs)
  • Periodic Safety Update Report (PSUR’s)
  • Individual Case Safety Report (ICSR) Processing
  • Safety Signal Management
  • Fully validated Pharmacovigilance Safety Database
    
    

Availability to Work

Europe, United Kingdom, Worldwide

Areas of Expertise

Standard Operating Procedures, Audit - Pharmacovigilance (GPvP), Audit - Post Marketing PV, Auditing Good Pharmacovigilance Practice, CRO, Good Pharmacoviglance Practice (GPvP), Pharmacovigilance (PV), Pharmacovigilance (GVP), Medical Devices, Medical Affairs

Contact Details

Sam Tipper
Peterson House, Middle River, Douglas, Isle of Man, EM2 1AL

Telephone: +44 (0) 1624 672777 

E-mail: sam.tipper@panacea.im

Website: www.panacea.im

Back to Register of Consultants